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Blue Button use by patients to access and share health record information using the Department of Veterans Affairs' online patient portal.
- Published in:
- Journal of the American Medical Informatics Association, 2014, v. 21, n. 4, p. 657, doi. 10.1136/amiajnl-2014-002723
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- Article
Use of Electronic Health Records in Disaster Response: The Experience of Department of Veterans Affairs After Hurricane Katrina.
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- American Journal of Public Health, 2007, v. 97, p. S136, doi. 10.2105/AJPH.2006.104943
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- Article
Health care implications of the Genetic Non-Discrimination Act: Protection for Canadians' genetic information.
- Published in:
- 2022
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- Publication type:
- journal article
Genetic education for primary care providers: Improving attitudes, knowledge, and confidence.
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- Canadian Family Physician / Médecin de Famille Canadien, 2009, v. 55, n. 12, p. e92
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- Article
AKBAR AND AURANGZEB-SYNCRETISM AND SEPARATISM IN MUGHAL INDIA A RE-EXAMINATION*.
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- Muslim World, 1969, v. 59, n. 2, p. 106, doi. 10.1111/j.1478-1913.1969.tb00479.x
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- Article
Managing the life cycle of electronic clinical documents.
- Published in:
- 2006
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- Publication type:
- journal article
Managing the Life Cycle of Electronic Clinical Documents.
- Published in:
- Journal of the American Medical Informatics Association, 2006, v. 13, n. 4, p. 438, doi. 10.1197/jamia.M1988
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- Publication type:
- Article
Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L769V Mutation in SCN4A.
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- Frontiers in Neurology, 2020, p. 1, doi. 10.3389/fneur.2020.00077
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- Article
17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD).
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- European Journal of Human Genetics, 2011, v. 19, n. 11, p. 1144, doi. 10.1038/ejhg.2011.97
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- Article
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.
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- Nature Genetics, 2006, v. 38, n. 7, p. 801, doi. 10.1038/ng1814
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- Article
Canadian guideline on genetic screening for hereditary renal cell cancers.
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- Canadian Urological Association Journal, 2013, v. 7, n. 9/10, p. 319, doi. 10.5489/cuaj.1496
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- Article
A Common Polymorphism in the Interleukin 8 Gene Promoter Is Associated with Clostridium difficile Diarrhea.
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- American Journal of Gastroenterology (Springer Nature), 2006, v. 101, n. 5, p. 1112, doi. 10.1111/j.1572-0241.2006.00482.x
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- Article
A retrospective review of 48 individuals, including 12 families, molecularly diagnosed with hereditary leiomyomatosis and renal cell cancer (HLRCC).
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- Familial Cancer, 2018, v. 17, n. 4, p. 615, doi. 10.1007/s10689-018-0076-4
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- Article
Similar values, different expectations: How do patients and providers view 'health' and perceive the healthcare experience?
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- Health Expectations, 2022, v. 25, n. 4, p. 1517, doi. 10.1111/hex.13493
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- Article
Investigation of Varicella-Zoster Virus Infection by Polymerase Chain Reaction in the Immunocompetent Host with Acute Varicella.
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- Journal of Infectious Diseases, 1991, v. 163, n. 5, p. 1016
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- Article
Primary care hypnotic and anxiolytic prescription: Reviewing prescribing practice over 8 years.
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- Journal of Family Medicine & Primary Care, 2016, v. 5, n. 3, p. 652, doi. 10.4103/2249-4863.197312
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- Publication type:
- Article
You Wrote it ... But Will Anybody Read it ?
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- Asia Pacific Journal of Human Resources, 1978, v. 16, n. 2, p. 37, doi. 10.1177/103841117801600207
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- Article
Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13C.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 4, p. 706, doi. 10.1002/ajmg.a.33884
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- Publication type:
- Article
Discordant phenotypes in a mother and daughter with mosaic supernumerary ring chromosome 19 explained by a de novo 7q36.2 deletion and 7p22.1 duplication.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 4, p. 885, doi. 10.1002/ajmg.a.33918
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- Publication type:
- Article
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
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- Human Mutation, 2008, v. 29, n. 9, p. 1125, doi. 10.1002/humu.20750
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- Article
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
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- Human Mutation, 2005, v. 26, n. 6, p. 513, doi. 10.1002/humu.20253
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- Article
Pre- and Postnatal Transplantation of Fetal Mesenchymal Stem Cells in Osteogenesis Imperfecta: A Two-Center Experience.
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- Stem Cells Translational Medicine, 2014, v. 3, n. 2, p. 255, doi. 10.5966/sctm.2013-0090
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- Article
Macrocephaly and developmental delay caused by missense variants in RAB5C.
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- Human Molecular Genetics, 2023, v. 32, n. 21, p. 3063, doi. 10.1093/hmg/ddad130
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- Article
Phenotypic heterogeneity associated with KIF21A: Two new cases and review of the literature.
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- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 3, p. 1, doi. 10.1002/ajmg.a.63455
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- Article
A 79‐kb paternally inherited 7q32.2 microdeletion involving MEST in a patient with a Silver‐Russell syndrome‐like phenotype.
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- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 8, p. 2421, doi. 10.1002/ajmg.a.62782
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- Article
Tatton‐Brown‐Rahman syndrome: Six individuals with novel features.
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 4, p. 673, doi. 10.1002/ajmg.a.61475
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- Article
Diagnostic clarity of exome sequencing following negative comprehensive panel testing in the neonatal intensive care unit.
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- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 7, p. 1688, doi. 10.1002/ajmg.a.38838
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- Article
Benchmarking outcomes in the Neonatal Intensive Care Unit: Cytogenetic and molecular diagnostic rates in a retrospective cohort.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 7, p. 1839, doi. 10.1002/ajmg.a.38250
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- Publication type:
- Article
An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequences.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 9, p. 2085, doi. 10.1002/ajmg.a.37128
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- Article
Atypical fibrodysplasia ossificans progressiva diagnosed by whole-exome sequencing.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 6, p. 1337, doi. 10.1002/ajmg.a.36969
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- Article
Multiple neurofibromas as the presenting feature of familial atypical multiple malignant melanoma (FAMMM) syndrome.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 6, p. 1425, doi. 10.1002/ajmg.a.35884
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- Article
Severe craniosynostosis in an infant with deletion 22q11.2 syndrome.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 1, p. 153, doi. 10.1002/ajmg.a.35491
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- Article
Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion.
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- Annals of Neurology, 1997, v. 41, n. 5, p. 675, doi. 10.1002/ana.410410518
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- Article
Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.
- Published in:
- 2016
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- Publication type:
- journal article